Gain of Chromosome 1q is associated with early progression in multiple myeloma patients treated with lenalidomide, bortezomib, and dexamethasone

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Timothy M. Schmidt
Benjamin G. Barwick
Nisha Joseph
Leonard T. Heffner
Craig C. Hofmeister
Leon Bernal
Madhav V. Dhodapkar
Vikas A. Gupta
David L. Jaye
Jiayi Wu
Subir Goyal
Zhengjia Chen
Lawrence H. Boise
Sagar Lonial
Ajay K. Nooka
Jonathan L. Kaufman
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[1] Emory University,Winship Cancer Institute, Department of Hematology and Medical Oncology
[2] Emory University,Department of Pathology and Laboratory Medicine
[3] Emory University,Department of Biostatistics & Bioinformatics, Rollins School of Public Health
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Gain of chromosome 1q (+1q) is commonly identified in multiple myeloma and has been associated with inferior outcomes. However, the prognostic implication of +1q has not been evaluated in the setting of standard triplet regimens. We retrospectively analyzed 201 consecutive patients with newly diagnosed myeloma who received induction with lenalidomide, bortezomib, and dexamethasone (RVD) and were tested for +1q at diagnosis by fluorescent in-situ hybridization. Patients with +1q (n = 94), compared to those without +1q (n = 107), had shorter median progression-free survival (PFS) (41.9 months vs 65.1 months, p = 0.002, HR = 1.90) and overall survival (median not reached (NR) for either arm, p = 0.003, HR 2.69). In subgroup analyses, patients with co-occurring +1q and t(4;14), t(14;16) or del(17p) or with 4 or more copies of 1q had significantly worse PFS (25.1 months and 34.6 months, p < 0.001 and p = 0.0063, respectively), whereas patients with three copies and no other high-risk cytogenetic abnormalities had no significant difference in PFS. These data suggest that when treated with RVD induction, patients with +1q should be considered at very high risk for early progression in multiple myeloma when ≥4 copies are detected or in the context of other high-risk cytogenetic abnormalities.
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